|Publication number||US8156888 B2|
|Application number||US 12/708,425|
|Publication date||Apr 17, 2012|
|Filing date||Feb 18, 2010|
|Priority date||Aug 26, 2005|
|Also published as||US7687098, US8192835, US20100206228, US20100211183, US20120269956|
|Publication number||12708425, 708425, US 8156888 B2, US 8156888B2, US-B2-8156888, US8156888 B2, US8156888B2|
|Original Assignee||Charlie W. Chi|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (22), Non-Patent Citations (1), Classifications (19), Legal Events (2)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation application of and claims priority under 35 U.S.C. §120 to U.S. patent application Ser. No. 11/212,977, now U.S. Pat. No. 7,687,098, entitled Chemical Mechanical Vapor Deposition Device for Production of Bone Substitute Material, filed Aug. 26, 2005, and which is hereby incorporated by reference in its entirety as though fully set forth herein.
This application is also related to co-pending U.S. patent application Ser. No. 12/708,438, entitled Chemical Mechanical Vapor Deposition Device for Production of Bone Substitute Material, filed on Feb. 18, 2010, and which is hereby incorporated by reference in its entirety as though fully set forth herein.
This invention relates to production of calcium phosphate mineral-based bone substitute material using a chemical solution spray deposition device that accommodates porous and composite laminar structures with reinforced biocompatible polymer fibers in order to encourage new bone growth as well as to provide mechanical strength and rigidity comparable to natural bone.
Bone is an organ composed of hard living tissue providing structural support to the body—it serves as scaffolding. A hard matrix of calcium salts is deposited around protein fibers. Minerals make bone rigid and protein (collagen) provides strength and elasticity. Bone is made of about 70 percent mineral and 30 percent of organic matrix. In an adult, bone engages in a continuous cycle of breaking down and rebuilding. Bone absorbing cells, called osteoclasts, break down bone and discard worn cells. After a few weeks, the osteoclasts disappear, and osteoblasts come to repair the bone. During the cycle, calcium and other minerals are withdrawn from the blood and deposited on the damaged bone surface. The outer layer of bone is called cortical bone; 80 percent of skeletal bone mass is cortical bone. Cancellous bone is an inner spongy structure that resembles honeycomb and accounts for 20 percent of bone mass. The shape of bone is described as long, short, flat, or irregular. The shape is further classified as axial or appendicular. Axial bones are protective. For example, spinal vertebrae protect the spinal cord. Appendicular bones are the limbs. Although there many shapes and sizes of skeletal bone, the bones that make up the spinal column are unique.
Cortical bone is a natural composite which exhibits a rich hierarchical structure. On the microstructural level are the osteons, which are large hollow fibers (about 200 microns in diameter) composed of concentric lamellae and pores. The lamellae are built from fibers, and the fibers contain fibrils. At the ultra-structural level, the fibers are a composite of the mineral hydroxyapatite (HAP) and the protein collagen. These specific structural features are associated with various physical properties. Stiffness of bone arises from the composite structure of mineral crystals and protein fibers. Visco-elastic properties result from slip at bone cement lines between osteon. The cement lines serve as weak interfaces to impart a degree of toughness to bone. As for pores, the lacunae are ellipsoidal pores, which provide space for the osteocytes, the living cells of bone. The pore structure of bone is essential in maintaining its viability and consequently its ability to adapt to mechanical stress. The processes of bone formation (osteogenesis) are involved with osteoinduction and osteoconduction. Osteoconduction is defined as the ability to stimulate the attachment, migration, and distribution of vascular and osteogenic cells within the graft material. Osteoinduction is defined as the ability to stimulate the proliferation and differentiation of pluripotent mesenchymal stem cells. The physical characteristics that affect the graft's osteoconductive activity include porosity, pore size, and three-dimensional architecture. In addition, direct biochemical interactions between matrix protein and cell surface receptors play a major role in the host's response to the graft material. The ability of a graft material to independently produce bone is termed its direct osteogenic potential. To have direct osteogenic activity, the graft preferably contains cellular components that directly induce bone formation.
Natural bone grafts have been extensively used to promote new bone growth (osteogenesis) in the orthopedic industry. Natural bone mineral is fundamentally a mixture of amorphous and crystalline calcium phosphate of HAP (hydroxyapatite) with Ca/P ratio of around 1.6. Natural bone grafts are associated with problems such as limited availability and risky recovery procedure for the autogenous bone, and risks of viral transmission and immune reaction for allograft bone from a cadaver. Consequently, biocompatible matrices are currently being developed to stimulate bone formation via osteoconduction and to promote osteoinduction by using osteogenic growth factors. The biocompatible material should satisfy the following: 1) incorporation and retaining of mesenchymal cells in tissue culture, 2) rapid induction of fibrilvascular invasion from the surrounding tissues, 3) having significant osteoconductive properties with the host bone, 4) no significant immune responses, 5) biomechanical properties similar to normal bone, 6) biodegradable properties with an absorption rate parallel to the rate of new bone deposition, and 7) sites with noncovalently binding osteogenic biomolecules to enhance osteoinduction. Numerous polymeric systems have been studied, including poly-α-hydroxy esters, polydioxanone, propylene fumarate, poly-ethylene glycol, poly-orthoesters, polyanhydrides, etc. These systems have the advantages of being already approved for use in humans and are available with varying porosities in any three-dimensional shape, and have been shown to be an excellent substrate for cellular or bioactive molecule delivery. Other types of materials include HAP (hydroxyapatite) and β-TCP (tricalcium phosphate). They have been the two most intensely studied materials for bone repair and regeneration. Their most unique property is chemical similarity to the mineralization phase of bone. This similarity accounts for their osteoconductive potential and excellent biocompatibility. Both HAP and β-TCP have been shown to be excellent carriers of osteoinduction growth factors and osteogenic cell population. However, by and large, metal, ceramic or polymer materials that have been introduced for bone substitutes have been substantially denser, heavier and significantly stiffer than natural bone although some ceramic materials exhibit similar chemical properties. Natural bone fails gradually when stressed under high compression. By contrast, bone substitute ceramic materials commonly show sudden and catastrophic failure under compression, because most of the bone substitute materials individually lack the several areas of biomechanical properties of natural bone, such as elasticity, viscoelasticity and lamellar structural properties.
What is needed is a calcium phosphate-based bone substitute material, and method of fabrication thereof, that is biocompatible with natural bone, is resorbable for osteogenesis, is rigid, is elastic with reinforced biocompatible polymer fibers, is viscoelasticity through use of multi-layered laminar structures, has controlled porosity, and has pore size(s) comparable to natural bone. The bone substitute should be strong and tough enough to support the spinal column for spinal surgeries as well as many other orthopedic applications.
These needs are met by the invention, which provides a production device and manufacturing processes, for bone substitute material with excellent osteoconductive and osteoinductive characteristics, that perform chemical solution spray deposition (CSSD) method incorporated with fiber reinforcing, isostatic press. The production device and manufacturing processes presented here rationally simulate natural bone repairing and building processes under various mechanical stresses.
In order to simulate the processes of osteoblasts and osteoclasts in natural bone rebuilding or new bone formation, a chemical solution spray deposition method is presented. In this process, solutions, which include calcium and phosphate ions in separate containers, are mechanically and simultaneously sprayed into an isolated chamber with formation of significant number of small solution particles (500 nanometers to 20 micro meters) in a liquid state. One container contains saturated solution of calcium chloride (CaCl2 (aq)). The other container contains saturated solution of hydrogen phosphate (H3PO4 (aq)). Optionally, a third container can be added to contain saturated solution of hydrogen carbonate (H2CO3 (aq)). And finally, another container with distilled water is added into the system to control a degree of saturation during the chemical reaction, i.e., high and low supersaturated states. It is noted that the proportion of phosphate co-precipitated depends on the temperature, pH and the concentration of calcium co-precipitating chemicals.
where σ is the maximum surface density of phosphorus, A is the surface area of phosphorus molecule, and the function h varies between Ca 0.1 and 0.9. This relation predicts the ratio of calcium to phosphorus for chemical formation of calcium phosphates precipitation, leading to the control of pH, the optimal concentration and the desirable particle sizes of each chemical during the chemical solution spray process.
The next step is that the small particles are transported into another isolated chamber by a reciprocating piston motion. By applying appropriate pressure caused by the downward piston motion and temperature to the chamber, the solution particles with calcium ion collide with those with phosphate ion, which induces chemical reaction between calcium and phosphate ions in combination with water molecules to formulate various calcium phosphate precipitates, such as hydroxyapatite (HAP), tricalcium phosphate (TCP), octacalcium phosphate (OCP), and dicalcium phosphate dihydrate (DCDP). One of the equilibrium chemical reactions is expressed as:
The phosphorous contents of the minerals are very similar, and therefore accurate chemical analysis is required to distinguish between these minerals from changes in the solution composition during crystal growth. At high supersaturations, it is difficult to precipitate HAP alone because of the spontaneous formation of precursor phases, such as amorphous DCDP, TCP and OCP. At lower supersaturations, it has been found possible to nucleate HAP in pH conditions where the solutions are slightly under-saturated with respect to amorphous TCP and OCP. The shape growth curve can provide the process information of the percentage crystalline HAP growth on the seeds through progressive amorphous and precursor phases such as TCP, OCP and DCDP. More significantly, the ratio of crystalline to amorphous structures is closely related, not only to mechanical properties, but also to osteoconductive and osteoinductive activities during the fusion process with natural bone. The precipitates of calcium phosphate minerals in both amorphous and crystalline structures move to a final chamber and are finally deposited on the substrate surface, preferably, calcium carbonate. They are accumulated in thickness with the formation of porous structures. The pore size is determined by the solution particle size during the spraying process. More significantly, the production device presented here enables control of various ratios of amorphous to crystalline structures in calcium phosphate minerals by adjusting pressure, temperature, a solution particle size, concentration of chemicals and amount of solvent (distilled water), i.e., pH, based on the shape growth curve.
For the simulation of mechanical properties of protein, which provides elastic property and strength of natural bone, biocompatible polymer fibers, preferably, PEEK (polyetheretherketone), are added to reinforce calcium phosphate minerals during the calcium phosphate mineral deposition. Biocompatible polymers, such as PEEK, have excellent flexural, impact and tensile characteristics. Especially, PEEK is insoluble in all common solvents and, being crystalline, is extremely resistant to attack by a very wide range of organic and inorganic chemicals. It has excellent hydrolysis resistance in boiling water (autoclave sterilization) and good radiation resistance (irradiation sterilization).
When a thin layer of calcium phosphate minerals fully reinforced by polymer fibers is observed, it undergoes an isostatic press process. The isostatic press process is used to simulate the new bone formation under various stresses in a human body. This process provides more compact structures between the calcium phosphate minerals and polymer fibers; furthermore, during the process, the pore size can be controlled in terms of isostatic pressure levels. The process is repeated to deposit additional thin layers until desired overall thickness is obtained inside the production device chamber. Consequently, stiffness of bone substitute arises from the composite structure of calcium phosphate minerals and polymer fibers. Viscoelastic properties can be obtained from slip lines between laminated thin layers of the calcium phosphate minerals.
The slip lines as weak interfaces can represent a degree of toughness and viscoelasticity to bone substitute material. This is an advantage using composite laminar structure. To further increase the compressive strength and rigidity of the bone substitute, thinner calcium carbonate mineral layers, compared to calcium phosphate mineral layers, can be deposited to simulate the natural bone cement slip lines. Also, in order to improve osteoinductive activities, blood vessels which nourish the tissue in natural bone (i.e., Haversian canals and Volkmann's canals) are simulated by introducing a mechanical through-hole device that allows incorporation of a finite number of through holes perpendicular or parallel to laminated directions depending on the application. These features in combination with bone morphogenetic protein (BMP) can significantly increase an osteoinductive activity. Furthermore, extracellular matrix scaffolds (ECM) can be added in combination with the polymer fibers or into transition layers (calcium carbonate layers) between the laminated calcium phosphate mineral layers. Various ECM proteins including collagen, laminin, fibronectin, and glycodaminiglcans, can be added for excellent biological scaffolds. These proteins have the advantages of supporting the migration and differentiation of osteoblastic progenitor cells, facilitate the binding of growth factors responsible for osteogenesis, and resorbing within a reasonably short period of time. At the cellular level, ECM molecules exhibit a variety of activities, including acting as a substrate for cell migration, an adhesive for cell anchorage, a ligand for ions, growth factors, and other bioactive agents. ECM molecules are ideal to form layers or substrates for cell delivery to provide high local concentrations of osteoinductive biomolecules.
The bone substitute material must have a ratio of calcium to phosphate of around 1.6 and at least 70 MPa of compressive strength with slight viscoelastic behavior. In order to further increase compressive strength of bone substitute material, the bulk of bone substitute material can undergo an additional isostatic press process, preferably, with saline solution. The bulk of polymer fiber reinforced calcium phosphate minerals with controlled porosity and composite laminated structures can be fabricated for many different applications in the orthopedic industry. For instance, the bone substitute material can be machined and fabricated for spinal fusion implants, i.e., lumbar and cervical inter-body fusion implants. Consequently, in combination with bone morphogenetic protein (BMP), the bone substitute implants are strong and tough enough to support spinal column with bio-safety and eventually fused with vertebral end bodies.
The invention is described with reference to the following figures:
The invention provides production of a bone substitute material using chemical solution spray deposition (CSSD) and isostatic press processes with reinforced plastic fibers, preferably PEEK, resulting in bone substitute having composite laminated structures with controlled porosity. In order to increase toughness and elastic behavior of bone substitute material comparable to natural bone, the composite laminar structure is introduced with reinforced polymer fibers. In order for bone substitute material to have high compressive strength in load bearing applications, calcium phosphate mineral is deposited and forms a layer with an option of inclusion of calcium carbonate mineral into the calcium phosphate mineral. Another option is that calcium carbonate forms one or more separate thin layers between the calcium phosphate layers. The high compressive strength of calcium carbonate material compared to calcium phosphate can provide additional rigidity of the bone substitute material. In case of any crack formed in a calcium phosphate layer, the calcium carbonate layer combined with polymer fibers can prevent micro cracks from further propagation. On the other hand, the calcium carbonate thin layer can provide the viscoelastic property similar to natural bone cement in bone lamellar structures.
To present the production device 101 in further detail, the overall production processes can be divided into five different processes: 1) vacuum process; 2) chemical solution spray process; 3) chemical reaction process; 4) deposition process; and 5) substantially isostatic press process. As shown in
As shown in
As soon as an optimal amount of chemicals is sprayed into the primary chamber 102, the chemical reactions proceed. Each solution particle moves freely inside the primary chamber 102 and collides with other particles. However, in order to accelerate the chemical reaction process and to promote highly homogenous precipitation, the piston 103 moves downward and pushes the chemical solution particles 401 into the secondary chamber 111, as shown in
Once the optimal conditions including the duration of chemical reactions are met, the valve 112 and the pressure cover 118 are open and the precipitates distribute uniformly adjacent to the bottom of the device (top surface of calcium carbonate substrate), shown in
A different approach from that illustrated in
Prior to the isostatic press process, the calcium phosphate minerals in combination with calcium carbonate are accumulated on the bottom of the third chamber. Due to the characteristics of the chemical solution spray deposition shown in
Finally, the vacuum process is repeated as shown in
As shown in
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4349518||Apr 27, 1981||Sep 14, 1982||Gte Products Corporation||Method of making high purity calcium hydrogen phosphate dihydrate|
|US4407262 *||Mar 2, 1981||Oct 4, 1983||Les Fabriques D'assortiments Reunies S.A.||Wafer dicing apparatus|
|US4702930||Nov 4, 1985||Oct 27, 1987||Battelle-Institute E.V.||Method of producing implantable bone replacement materials|
|US5188670||Apr 17, 1991||Feb 23, 1993||Norian Corporation||Apparatus for hydroxyapatite coatings of substrates|
|US5486365||Jul 8, 1994||Jan 23, 1996||Fuji Chemical Industry Co., Ltd.||Calcium hydrogen phosphate, a method for preparing it, and an excipient utilizing it|
|US5593741 *||Jun 28, 1995||Jan 14, 1997||Nec Corporation||Method and apparatus for forming silicon oxide film by chemical vapor deposition|
|US5728425 *||Mar 9, 1993||Mar 17, 1998||Fujitsu Limited||Method for chemical vapor deposition of semiconductor films by separate feeding of source gases and growing of films|
|US5730801 *||Aug 23, 1994||Mar 24, 1998||Applied Materials, Inc.||Compartnetalized substrate processing chamber|
|US6129928||Sep 4, 1998||Oct 10, 2000||Icet, Inc.||Biomimetic calcium phosphate implant coatings and methods for making the same|
|US6183564 *||Nov 12, 1998||Feb 6, 2001||Tokyo Electron Limited||Buffer chamber for integrating physical and chemical vapor deposition chambers together in a processing system|
|US6296667||Oct 1, 1997||Oct 2, 2001||Phillips-Origen Ceramic Technology, Llc||Bone substitutes|
|US6384196||Mar 24, 1999||May 7, 2002||Merck Patent Gesellschaft||Process for the preparation of mineralized collagen fibrils and their uses as bone substitute material|
|US6409837 *||Jan 13, 1999||Jun 25, 2002||Tokyo Electron Limited||Processing system and method for chemical vapor deposition of a metal layer using a liquid precursor|
|US6455098 *||Mar 8, 2001||Sep 24, 2002||Semix Incorporated||Wafer processing apparatus and method|
|US6613105 *||Dec 23, 1999||Sep 2, 2003||Micron Technology, Inc.||System for filling openings in semiconductor products|
|US6840961||Dec 21, 2001||Jan 11, 2005||Etex Corporation||Machinable preformed calcium phosphate bone substitute material implants|
|US6846853||Jul 16, 2002||Jan 25, 2005||Osteotech, Inc.||Calcium phosphate bone graft material, process for making same and osteoimplant fabricated from same|
|US7390335||Apr 6, 2005||Jun 24, 2008||American Dental Association Foundation||Nanostructured bioactive materials prepared by spray drying techniques|
|US7687098||Aug 26, 2005||Mar 30, 2010||Charlie W. Chi||Chemical mechanical vapor deposition device for production of bone substitute material|
|US20050226939||Apr 7, 2004||Oct 13, 2005||National University Of Singapore||Production of nano-sized hydroxyapatite particles|
|US20070059379||May 24, 2004||Mar 15, 2007||Thomas Gerber||Inorganic resorbable bone substitute material|
|US20100211183||Feb 18, 2010||Aug 19, 2010||Charles Chi||Chemical Mechanical Vapor Deposition Device for Production of Bone Substitute Material|
|1||Tadic et al., "Continuous synthesis of amorphous carbonated apatites," Biomaterials, vol. 23, pp. 2553-2559, 2002.|
|U.S. Classification||118/300, 118/733, 118/732|
|International Classification||C23C16/00, B05B7/00|
|Cooperative Classification||C23C18/1204, Y10T428/25, C23C18/1245, Y10T428/254, A61F2002/30784, A61F2/28, A61F2/3094, A61F2002/30986, A61F2002/30971, A61F2/30965, A61F2310/00293|
|European Classification||C23C18/12C, A61F2/28, C23C18/12G6|
|May 12, 2010||AS||Assignment|
Owner name: CHI, CHARLIE W., CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:OTISMED CORPORATION;REEL/FRAME:024375/0898
Effective date: 20080722
Owner name: OTISMED CORPORATION, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CHI, CHARLIE W.;REEL/FRAME:024375/0788
Effective date: 20070110
|Sep 30, 2015||FPAY||Fee payment|
Year of fee payment: 4